Drug Safety Associate

About the Role and Company

Join a leading global professional services firm based in Bengaluru, India, specializing in digital, cloud, and security capabilities across over 40 industries including life sciences. We offer extensive services from Strategy and Consulting to Technology and Operations, powered by a vast network of centers globally.

Pharmacovigilance and Drug Safety Responsibilities

Within our Life Sciences R&D vertical, you will focus on supporting clinical research, regulatory affairs, and pharmacovigilance activities to assist top biopharma companies in improving patient outcomes through scientific and patient insight convergence. Your work will ensure medication safety by monitoring adverse events, assessing risks, and complying with regulatory standards.

• Manage identification and creation of safety reports (ICSRs), perform data entry and MedDRA coding.
• Process cases, submit them, and conduct follow-ups within the safety database based on client and global regulatory protocols.
• Work in a team environment with guidance on routine tasks and moderate instructions for new assignments.
• Solve routine problems primarily by referring to established guidelines and precedents.
• Communicate mainly with your immediate team and supervisor.
• Contribute as an individual team member with a defined scope of responsibilities.
• Be prepared for rotational shift work as part of your role.

Qualifications and Experience

Ideal candidates hold a Bachelor of Science or Bachelor of Pharmacy degree with 1 to 3 years of experience in pharmacovigilance operations focusing on drug safety surveillance.